We consider a two-competitor/one-prey model in which both competitors exhibit a general functional response and one of the competitors exhibits a density-dependent mortality rate. It is shown that the two competitors can coexist upon the single prey.As an example, we consider a two-competitor/one-prey model with a Holling II functional response. Our results demonstrate that density-dependent mortality in one of the competitors can prevent competitive exclusion. Moreover, by constructing a Liapunov function, the system has a globally stable positive equilibrium.
Lyapunov functions are given to prove the global asymptotic stability of a large class of predator-prey models, including the ones in which the intrinsic growth rate of the prey follows the Ricker-law or the Odell generalization of the logistic law, and the functional predator response is of Holling type.
An acidic peroxidase (EC 1.11.1.7) produced by cell suspension cultures of Cassia didymobotrya (wild senna) was purified from culture medium collected on the 29th day. The enzyme was shown to be a glycoprotein with a pI of 3.5, a molecular mass of approx. 43 kDa by SDS/PAGE and 50 kDa by gel filtration. The N-terminal sequence was very similar to those of other plant peroxidases. The peroxidase was characterized by a high specificity towards coniferyl alcohol and other natural phenolics such as guaiacol and ferulic and caffeic acids. These findings suggest that the enzyme is involved in lignification processes of the cell wall. Moreover, the enzyme was able to catalyse the oxidation of 4,3',4'-trihydroxychalcone and 4, 3',4'-trihydroxy-3-methoxychalcone to the corresponding 3, 3'-biflavanones, as mixtures of racemic and meso forms.
Resorcinarene octamethyl ethers, bearing carboalkyloxy groups in the side chains, have been shown to interact with FeIII in organic media. 1H‐NMR studies, carried out using GaIII instead of FeIII, suggest that these systems have two active sites of interaction, the first located at the aromatic moiet and the other in the vicinity of the carbonyl groups. As a confirmation of this, resorcinarenes without carbonyl groups in the side chains have been found to exhibit only one active site. Notably, in the latter case the interaction results in configurational changes.
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